A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1925



Internal ID15199802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88498349..88543493hg38UCSC Ensembl
Outerchr16:88564757..88609901hg19UCSC Ensembl
Outerchr16:87092258..87137402hg18UCSC Ensembl
Outerchr16:87092258..87137402hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3845145
hg1945145
hg1845145
hg1745145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7295
SamplesNA12156
Known GenesZFPM1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv1925
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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